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Development of liquid chromatographic method for the analysis of dabigatran etexilate mesilate and its ten impurities supported by quality-by-design methodology
(Elsevier Science BV, Amsterdam, 2015)
In this paper, the development of reversed-phase liquid chromatographic method for the analysis of dabigatran etexilate mesilate and its ten impurities supported by quality by design (QbD) approach is presented. The defined ...
Densitometric determination of conjugated oestrogens in the raw material and in pharmaceutical preparations
(Journal of Pharmaceutical and Biomedical Analysis, 1990)
A densitometric method for determination of complex mixtures of conjugated oestrogens in raw material and tablets was developed. The proposed procedure comprised hydrolysis of sodium sulphate esters of oestrone, equilin, ...
Spectrophotometric determination of mesterolone in tablets using 3-acetylaminobenzaldehydethiosemicarbazone
(Journal of Pharmaceutical and Biomedical Analysis, 1989)
High-performance liquid chromatographic method for the determination of bumetanide in pharmaceutical preparations
(Journal of Pharmaceutical and Biomedical Analysis, 1989)
High performance thin layer chromatography (HPTLC) and high performance liquid chromatography (HPLC) for the qualitative and quantitative analysis of Calendula officinalis-Advantages and limitations
(Elsevier Science BV, Amsterdam, 2014)
Chromatography techniques such as HPTLC and HPLC are commonly used to produce a chemical fingerprint of a plant to allow identification and quantify the main constituents within the plant. The aims of this study were to ...
Application of Analytical Quality by Design concept for bilastine and its degradation impurities determination by hydrophilic interaction liquid chromatographic method
(Elsevier Science BV, Amsterdam, 2016)
This paper deals with the development of hydrophilic interaction liquid chromatographic (HILIC) method for the analysis of bilastine and its degradation impurities following Analytical Quality by Design approach. It is the ...
Use of palladium(II) chloride as colour-forming reagent in determination of pralidoxime chloride in water and tablets
(Journal of Pharmaceutical and Biomedical Analysis, 1988)
Pralidoxime chloride (PAM-2Cl) has been determined spectrophotometrically in Britton-Robinson buffer solution at pH = 6.45; the method is based on measurement of the absorbance of the Pd(II)-pralidoxime complex at 327 nm. ...
Quality by Design approach in the development of hydrophilic interaction liquid chromatographic method for the analysis of iohexol and its impurities
(Elsevier Science BV, Amsterdam, 2015)
This study presents the development of hydrophilic interaction liquid chromatographic method for the analysis of iohexol, its endo-isomer and three impurities following Quality by Design (QbD) approach. The main objective ...
Potentiometric investigation of the stability of palladium(II) complex of pralidoxime chloride in aqueous solution
(Journal of Pharmaceutical and Biomedical Analysis, 1990)
The formation of a complex between palladium(II) chloride and pralidoxime chloride (PAM-2Cl) has been studied by means of potentiometric pH measurements. The real stability constant of the complex in aqueous medium of ionic ...
Spectrophotometric investigation of complex formation of an oxime PAM-4Cl with palladium(II) and its analytical application
(Journal of Pharmaceutical and Biomedical Analysis, 1990)
The colour reaction of 4-hydroxyiminomethyl-1-methylpyridinium chloride (PAM-4Cl) and palladium(II) chloride has been investigated. The optimum reaction conditions, spectral characteristics, conditional stability constant ...